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International Journal of Clinical & Laboratory Research
|
January 1, 1994
A new method for direct analysis of polymerase chain reaction-amplified human papillomavirus using DNA enzyme immunoassay
F Sangiuolo, L De Santis, A Cavicchini, et al.
Biochemistry and Molecular Biology International
|
October 27, 2009
Recombinant CTFR detection in CF tracheal epithelial cells following in vitro liposomeme-mediated gene transfer
A Colosimo, S Scarpino, F Sangiuolo, et al.
Human Heredity
|
September 1, 1993
Identification of three novel cystic fibrosis mutations in a sample of Italian cystic fibrosis patients
M P Audrézet, G Novelli, B Mercier, et al.
Transplantation Proceedings
|
December 1, 1996
Liver pretransplant patient management with transjugular-portosystemic shunt
R Cortesini, M Rossi, P De Simone, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD
|
August 5, 2008
Short-term mortality risk in children and young adults with type 1 diabetes: the population-based Registry of the Province of Turin, Italy
G Bruno, F Cerutti, F Merletti, et al.
Biochemistry and Molecular Biology International
|
February 1, 1993
Failure in detecting mRNA transcripts from the mutated allele in myotonic dystrophy muscle
G Novelli, M Gennarelli, G Zelano, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
September 1, 1992
[The correlation between the genotype and the clinical expression of cystic fibrosis]
V Lucidi, G Novelli, M Castro, et al.
Human Mutation
|
April 24, 1999
Identification of five new mutations and three novel polymorphisms in the muscle chloride channel gene (CLCN1) in 20 Italian patients with dominant and recessive myotonia congenita. Mutations in brief no. 118. Online
F Sangiuolo, A Botta, A Mesoraca, et al.
Journal of Endocrinological Investigation
|
May 1, 1994
Male hypogonadism in myotonic dystrophy is related to (CTG)n triplet mutation
I Mastrogiacomo, E Pagani, G Novelli, et al.
Gastroenterology
|
September 15, 2007
Interleukin-23R Arg381Gln is associated with susceptibility to Crohn's disease but not with phenotype in an Italian population
P Borgiani, C Perricone, C Ciccacci, et al.
Page
of 33
Search research articles
Search
Showing results (151-160 of 330) with videos related to
Sort By:
Page
of 33
International Journal of Clinical & Laboratory Research
|
January 1, 1994
A new method for direct analysis of polymerase chain reaction-amplified human papillomavirus using DNA enzyme immunoassay
F Sangiuolo, L De Santis, A Cavicchini, et al.
Biochemistry and Molecular Biology International
|
October 27, 2009
Recombinant CTFR detection in CF tracheal epithelial cells following in vitro liposomeme-mediated gene transfer
A Colosimo, S Scarpino, F Sangiuolo, et al.
Human Heredity
|
September 1, 1993
Identification of three novel cystic fibrosis mutations in a sample of Italian cystic fibrosis patients
M P Audrézet, G Novelli, B Mercier, et al.
Transplantation Proceedings
|
December 1, 1996
Liver pretransplant patient management with transjugular-portosystemic shunt
R Cortesini, M Rossi, P De Simone, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD
|
August 5, 2008
Short-term mortality risk in children and young adults with type 1 diabetes: the population-based Registry of the Province of Turin, Italy
G Bruno, F Cerutti, F Merletti, et al.
Biochemistry and Molecular Biology International
|
February 1, 1993
Failure in detecting mRNA transcripts from the mutated allele in myotonic dystrophy muscle
G Novelli, M Gennarelli, G Zelano, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
September 1, 1992
[The correlation between the genotype and the clinical expression of cystic fibrosis]
V Lucidi, G Novelli, M Castro, et al.
Human Mutation
|
April 24, 1999
Identification of five new mutations and three novel polymorphisms in the muscle chloride channel gene (CLCN1) in 20 Italian patients with dominant and recessive myotonia congenita. Mutations in brief no. 118. Online
F Sangiuolo, A Botta, A Mesoraca, et al.
Journal of Endocrinological Investigation
|
May 1, 1994
Male hypogonadism in myotonic dystrophy is related to (CTG)n triplet mutation
I Mastrogiacomo, E Pagani, G Novelli, et al.
Gastroenterology
|
September 15, 2007
Interleukin-23R Arg381Gln is associated with susceptibility to Crohn's disease but not with phenotype in an Italian population
P Borgiani, C Perricone, C Ciccacci, et al.
Page
of 33